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BabyScreen+ newborn screening v1.114 PKLR Tommy Li Added phenotypes Pyruvate kinase deficiency, MIM#266200 for gene: PKLR
BabyScreen+ newborn screening v0.1710 PKLR Zornitza Stark Tag treatable tag was added to gene: PKLR.
Tag metabolic tag was added to gene: PKLR.
BabyScreen+ newborn screening v0.1569 PKLR Zornitza Stark Marked gene: PKLR as ready
BabyScreen+ newborn screening v0.1569 PKLR Zornitza Stark Gene: pklr has been classified as Green List (High Evidence).
BabyScreen+ newborn screening v0.1569 PKLR Zornitza Stark Publications for gene: PKLR were set to
BabyScreen+ newborn screening v0.1568 PKLR Zornitza Stark edited their review of gene: PKLR: Changed publications: 32702739
BabyScreen+ newborn screening v0.1568 PKLR Zornitza Stark changed review comment from: ranging from fetal hydrops and symptomatic anemia requiring lifelong transfusions to fully compensated hemolysis.; to: Established gene-disease association.

Severity ranges from fetal hydrops and symptomatic anaemia requiring lifelong transfusions to fully compensated haemolysis.

Treatment: Mitapivat. Red cell transfusions.

For review.
BabyScreen+ newborn screening v0.1568 PKLR Zornitza Stark edited their review of gene: PKLR: Changed phenotypes: Pyruvate Kinase deficiency, MIM# 266200; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.1568 PKLR Zornitza Stark reviewed gene: PKLR: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
BabyScreen+ newborn screening v0.0 PKLR Zornitza Stark gene: PKLR was added
gene: PKLR was added to gNBS. Sources: BeginNGS,BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: PKLR was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: PKLR were set to Pyruvate kinase deficiency, MIM#266200